Theralase(R) Demonstrates Effectiveness Of X-Ray-Activated Drug
Theralase® was unable to attend the presentation of the poster in person titled, " Rutherrin® Activated by Radiation Therapy Induces Synergistic Tumor Regression through Direct Destruction and Immune Activation in Multiple Preclinical Cancer Models."
The abstract has been published in the International Journal of Radiation Oncology - Biology - Physics at the following link:
Rutherrin® Activated by Radiation Therapy and Synergistic Tumor Regression through Direct Destruction and Immune Activation in Multiple Preclinical Cancer Models - ScienceDirect
The full poster is available at the following link:
Research Publications | Theralase Technologies Inc. - Theralase Technologies
 
The study evaluated Theralase®'s lead drug formulation,  Rutherrin® (a ruthenium-based small molecule formulated with recombinant human transferrin), activated by radiation therapy in a number of preclinical cancer models; including, glioblastoma multiforme (a deadly form of brain cancer), lung cancer (most common cancer), colorectal cancer (third most common) and lymphoma (seventh most common).
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Key Findings:
-    Enhanced Tumor Destruction: Radiation-activated Rutherrin® achieved a  100-fold increase in cancer cell kill versus radiation therapy alone
 
-    Oxidative and Immune Mechanisms: Rutherrin® increased  Reactive Oxygen Species ("  ROS ") production and stimulated  immune-related cytokine and chemokine expression, driving both immediate and immune-mediated cancer cell death
 
-    Overcoming Resistance: The compound modulated  drug efflux pathways, helping overcome mechanisms associated with multidrug and radiation resistance
 
-    Durable Immune Memory: In vivo, Rutherrin® combined with radiation induced  complete tumor regression in colorectal models and provided  long-term protection against tumor rechallenge
 
-    Tumor Selectivity and Survival: In GBM models, Rutherrin® demonstrated  >10-fold preferential tumor uptake over healthy brain tissue and, in both GBM and lung models, significantly  prolonged survival compared to radiation alone.
 
These key findings support Rutherrin® as a promising addition to radiation therapy, capable of improving local tumor control, overcoming treatment resistance and stimulating systemic immunity.
Mark Roufaiel, Ph.D., Research Scientist at Theralase® stated, "The preclinical research has demonstrated the utility of X-ray-activated Rutherrin® as a preferred addition to radiation therapy to increase efficacy, improve local tumor control, overcome treatment resistance and stimulate systemic immunity."
Arkady Mandel , M.D., Ph.D., D.Sc., Chief Scientific Officer of Theralase®, added, "Next steps in our research program are to complete Good Laboratory Practice toxicology studies in 2026, paving the way for the launch of clinical development targeting GBM, NSCLC, pancreatic, lymphoma and colorectal cancers."
Roger DuMoulin-White, B.Sc., P.Eng., Pro., President and Chief Executive Officer of Theralase®, stated, "We are proud to share our scientific research demonstrating Rutherrin®'s unique characteristics in the destruction of cancer. The patented compound amplifies radiation's direct cytotoxic effects, while stimulating a durable immune response, positioning it as a potential breakthrough in the management of aggressive cancers."
About Theralase ® Technologies Inc.
Theralase® is a clinical stage pharmaceutical company dedicated to the research and development of light, radiation, sound and drug-activated small molecule compounds and their associated formulations with a primary objective of efficacy and a secondary objective of safety in the destruction of various cancers, bacteria and viruses, with minimal impact on surrounding healthy tissue.
Additional information is available at and .
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For More Information:Kristina Hachey, CPA
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SOURCE: Theralase Technologies Inc.
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